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Electra Therapeutics, Inc.

ETRAFDA catalysts, PDUFA dates & pipeline intelligence
$8.98
▲ +0.46 · +5.4%

Financials

Last updated
Revenue
R&D Expenses
Operating CF
Total Assets
Total Liabilities
Equity
Shares Out.
D/E Ratio
Dilution Watch
Quarterly Cash
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Volume
177.30 K
Value Traded
-
Short % Float
1.06%
Days to Cover
1.0
-2.92%Week
-20.88%1 Month
-32.23%3 Month
-32.23%6 Month

Cash Data

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  • Monthly Burn
  • Burn Trend
  • Dilution Risk
  • SEC Filing

Key Stats

Market Cap
563.65 M
EPS (TTM)
-
P/E Ratio
-
Ent. Value
-
Total Shares
62.77 M
Float Shares
38.52 M
Insiders
38.62%
Institutions
8.74%

Upcoming Catalysts

FDA decisions, readouts and PDUFA dates · scored by probability of approval

Catalyst Drug / Treatment Stage Prob. of Approval Description Drug Type Therapeutic Area Source
PDUFA
2026
Example Drug
Treatment for example condition requiring FDA review
Phase 3Small MoleculeOncology-
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Every FDA decision, readout and PDUFA date, with drug type, therapeutic area and a PoA score you can trade on.
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PoA blends historical approval base rates, trial design score and FDA review track record.

ETRA Catalyst Timeline

Dated clinical, regulatory and corporate events for Electra Therapeutics, Inc.

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Every PDUFA date, readout, approval and corporate move, tiered by market impact and updated daily.
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Past FDA Catalysts and PDUFA Decisions

How ETRA actually traded into and out of each decision

Date Drug Catalyst Stage Reaction Event Move % Best Trade %
-Example Drug Phase 3 data readout Phase 3
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Reaction: 30 trading days around the event · Event Move: close to close on decision day · Best Trade: peak run-up from entry 10 days before the decision

Drug Pipeline Intelligence

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Every scored asset with PTRS, rNPV, enrollment velocity and trial design quality.
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Clinical Trial Results

Readouts, endpoints and source filings for every ETRA program

Drug Name Indication Phase Date Trial Results SummaryTitleSource
Example Drug Example indication for clinical evaluationPhase 32025-12-01The study met its primary endpoint demonstrating statistically significant improvement.Read MorePhase 3 Study Results AnnouncementRead More
Scroll for more · summaries link to the source press release
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Inside Trades

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Monthly insider buys and sells against the stock price, with the insider sentiment reading.
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InsiderSideSharesPriceValueDate
ORBIMED ADVISORS LLCDirector, 10% OwnerBuy 333,333 5,126,891 held$15.00 09/21/2026
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Hedge Fund 13F Activity

Fund % of Portfolio Current MV Shares Owned Activity
No hedge fund reported a 13F position in ETRA for Q2 2026.
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Every 13F position with quarter over quarter share flow and average entry price.
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Shares held by hedge funds each quarter, and who bought or sold.

ETRA Institutional Ownership Trends

ETRA Short Interest

Shares sold short, counted twice a month.

1.06%
Short % of Float
of tradable shares sold short
409.4K
Shares Sold Short
-41.7% vs prior count
1.0 Low
Days to Cover
trading days of normal volume to buy every short share back
516.1K
Avg Daily Volume
the average used for days to cover
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Two years of days to cover and shares sold short, with every count and its change.
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Options Data

Option Volume

Open Interest
Call OI
Put OI
Put-Call Ratio
OI 30-day avg
Today vs avg
Option Volume
Call Vol
Put Vol
Put-Call Ratio
Vol 30-day avg
Today vs avg

Option Chain Statistics

ExpiryCall VolPut VolVol P/CCall OIPut OIOI P/CIV CallIV Call OI-WtdIV Call Vol-WtdIV PutIV Put OI-WtdIV Put Vol-Wtd
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Per-expiry call and put volume, open interest, put-call ratios and implied volatility.
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Real-Time Option Chain

CallsStrikePuts
LastVolOILastVolOI
No data available
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Live calls and puts by strike: last price, volume and open interest for every expiry.
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Calls vs Puts by Expiry

CallsPutsLog scale
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Competitive positioning

How ETRA ranks across every disease it competes in

Competitive Position is a premium feature
See how ETRA ranks against every competitor across each disease it develops in: phase, best drug, trials and likelihood of approval.
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ETRA News

-ETRA
Sep 18, 2026
ETRAGeneral

Electra Therapeutics Announces Pricing of Upsized $350.0 Million Initial Public Offering

Electra Therapeutics has announced the pricing of its upsized initial public offering, raising approximately $350 million by offering 23,333,334 shares at $15.00 each. The shares are set to begin trading on Nasdaq under the ticker ETRA on September 18, 2026, with the offering expected to close on September 21, 2026. This funding will support the company's development of precision medicines for immune-mediated diseases and cancer.

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-ETRA
Sep 10, 2026
ETRAPhases

Electra Therapeutics Announces Initiation of a Phase 1 Trial of ELA822, a Novel SIRPγ-Specific Antibody Designed to Treat T Cell-Mediated Immune and Inflammatory Diseases

Electra Therapeutics has initiated a Phase 1 clinical trial for ELA822, a novel SIRPγ-specific monoclonal antibody aimed at treating T cell-mediated immune and inflammatory diseases. The trial will assess the safety, tolerability, and pharmacokinetics of ELA822 in healthy volunteers. Preclinical studies indicated that ELA822 effectively depletes activated T cells while sparing regulatory T cells, showing promise for chronic disease applications.

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-ETRA
Sep 9, 2026
ETRAGeneral

Electra Therapeutics Appoints Chris Clark, CFA, to Chief Financial Officer

Electra Therapeutics has promoted Chris Clark to Chief Financial Officer. Clark, who joined in December 2025, has over 20 years of experience in biopharmaceutical investments. His role will be crucial as the company advances its lead candidate, ipsoprubart, through global registrational programs and expands its clinical pipeline.

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-ETRA
May 5, 2026
ETRAPhases

Electra Therapeutics Announces First Patient Dosed in Phase 1 Study of Ipsoprubart (ELA026) in T Cell Malignancies

Electra Therapeutics has dosed the first patient in a Phase 1 study of ipsoprubart (ELA026) targeting T cell malignancies. This first-in-class therapy aims to selectively deplete pathological T cells and myeloid cells, building on previous positive results in lymphoma patients. The study will evaluate safety and efficacy in adults with relapsed or refractory conditions.

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-ETRA
Jan 5, 2026
ETRAConferences/Events

Electra Therapeutics to Present at 44th Annual J.P. Morgan Healthcare Conference

Electra Therapeutics will present at the 44th annual J.P. Morgan Healthcare Conference from January 12-15, 2026. CEO Kathy Dong will discuss the company's SIRP-targeted therapies, including ELA026, which is in pivotal studies for secondary hemophagocytic lymphohistiocytosis. The company is also advancing ELA822 for immunology and inflammation diseases.

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-ETRA
Dec 2, 2025
ETRAConferences/Events

Electra Therapeutics Presents SURPASS Pivotal ELA026 Study Design and Highlights the Critical Unmet Need in Secondary Hemophagocytic Lymphohistiocytosis (sHLH) at the ASH 2025 Annual Meeting

Electra Therapeutics will present the SURPASS Phase 2/3 study design for ELA026 at the ASH 2025 Annual Meeting. This investigational therapy targets secondary hemophagocytic lymphohistiocytosis (sHLH) and aims to address significant unmet needs in treatment. The study's findings underscore the life-threatening nature of sHLH and the limited effectiveness of current therapies.

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-ETRA
Oct 22, 2025
ETRAGeneral

Electra Therapeutics Announces $183 Million Series C Financing to Advance First-in-Class SIRP-Targeted Therapies for Immune Disorders and Cancer

Electra Therapeutics announced a $183 million Series C financing to support its lead candidate ELA026 in a pivotal trial for secondary hemophagocytic lymphohistiocytosis. The funding will also facilitate the expansion of ELA026 into hematologic cancers and advance the second pipeline program, ELA822.

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-ETRA
Oct 22, 2025
ETRAPhases

Electra Therapeutics Announces First Patients Dosed in the SURPASS Phase 2/3 Pivotal Study of ELA026 in Secondary Hemophagocytic Lymphohistiocytosis (sHLH)

Electra Therapeutics announced the dosing of the first patients in the SURPASS Phase 2/3 study for ELA026, targeting secondary hemophagocytic lymphohistiocytosis (sHLH). ELA026 aims to treat this life-threatening condition by depleting pathological immune cells. The study will assess safety and efficacy, with promising results from previous trials indicating high survival rates.

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-ETRA
Oct 22, 2025
ETRAFDA Updates

Electra Therapeutics Receives FDA Breakthrough Therapy and EMA Priority Medicines Designations for ELA026 in Secondary Hemophagocytic Lymphohistiocytosis (sHLH)

Electra Therapeutics announced that ELA026 has received FDA Breakthrough Therapy and EMA Priority Medicines designations for secondary hemophagocytic lymphohistiocytosis (sHLH). The drug demonstrated a 100% overall survival rate in a Phase 1b study for malignancy-associated HLH patients. Electra has initiated the SURPASS global pivotal trial to further evaluate ELA026's efficacy.

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-ETRA
Aug 4, 2025
ETRAFDA Updates

Electra Therapeutics Announces ELA026 Granted EMA Orphan Drug Designation for the Treatment of Secondary Hemophagocytic Lymphohistiocytosis (sHLH)

Electra Therapeutics announced that ELA026 has been granted Orphan Drug Designation by the EMA for treating secondary hemophagocytic lymphohistiocytosis (sHLH). This designation highlights the urgent need for effective therapies for this rare, life-threatening condition. ELA026 is designed to selectively deplete harmful immune cells, potentially improving patient outcomes.

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About Electra Therapeutics, Inc.

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